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Updated: Feb 8, 2026

Genome Engineering of Primary Human B Cells Using CRISPR/Cas9
Published on: November 3, 2020
The CRISPR/Cas9 System as a Tool to Engineer Chromosomal Translocation In Vivo
Taek-Chin Cheong1,2, Rafael B Blasco1,2, Roberto Chiarle3,4
1Department of Pathology, Boston Children's Hospital, Boston, MA, USA.
Abstract:
The CRISPR/Cas9 system has emerged as a powerful tool to edit the genome. Among many applications, the system generates the exciting possibility of engineering small and large portions of chromosomes to induce a variety of structural alterations such as deletions, inversions, insertions and inter-chromosomal translocations. Furthermore, the availability of viral vectors that express Cas9 has been critical to deliver the CRISPR/Cas9 system directly in vivo to induce chromosomal rearrangements. This review provides an overview of the state-of-the-art CRISPR/Cas9 technology to model a variety of rearrangements in vivo in animal models.
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